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IL-2-driven CD8+ T cell phenotypes: implications for immunotherapy

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F23%3A00578373" target="_blank" >RIV/68378050:_____/23:00578373 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388971:_____/23:00578373

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S1471490623001953?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S1471490623001953?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.it.2023.09.003" target="_blank" >10.1016/j.it.2023.09.003</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    IL-2-driven CD8+ T cell phenotypes: implications for immunotherapy

  • Original language description

    The therapeutic potential of interleukin (IL)-2 in cancer treatment has been known for decades, yet its widespread adoption in clinical practice remains limited. Recently, chimeric proteins of an anti-PD-1 antibody and suboptimal IL-2 variants were shown to stimulate potent antitumor and antiviral immunity by inducing unique effector CD8+ T cells in mice. A similar subset of cytotoxic T cells is induced by depletion of regulatory T cells (Tregs), suggesting IL-2 sequestration as a major mechanism through which regulatory T cells suppress activated CD8+ T cells. Here, we present our view of how IL-2-based biologicals can boost the antitumor response at a cellular level, and propose that the role of Tregs following such treatments may have been previously overestimated.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30102 - Immunology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Trends in Immunology

  • ISSN

    1471-4906

  • e-ISSN

    1471-4981

  • Volume of the periodical

    44

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    890-901

  • UT code for WoS article

    001101620100001

  • EID of the result in the Scopus database

    2-s2.0-85173934074